Search research articles
Contact Us
Filters
Showing results (1-10 of 15) with videos related to
Page
of 2
Sort By:
Current Protocols in Human Genetics
|
April 23, 2008
Single-strand conformation polymorphism analysis using capillary electrophoresis
Lars Allan Larsen, Michael Christiansen, Jens Vuust, et al.
Aesthetic Plastic Surgery
|
March 11, 2005
Adverse reactions to injectable soft tissue permanent fillers
Lise Christensen, Vibeke Breiting, Martin Janssen, et al.
Human Mutation
|
April 4, 2003
Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening
Paal Skytt Andersen, Cathrine Jespersgaard, Jens Vuust, et al.
Human Mutation
|
January 29, 2003
High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method
Paal Skytt Andersen, Cathrine Jespersgaard, Jens Vuust, et al.
Ugeskrift for Laeger
|
October 31, 2006
[Screening for fragile X syndrome. International experiences]
Jens Vuust, Lars Allan Larsen, Karen Grønskov, et al.
FEMS Microbiology Letters
|
September 29, 2004
Identification and molecular characterization of the gene encoding coli surface antigen 20 of enterotoxigenic Escherichia coli
Håvard Valvatne, Hans Steinsland, Harleen M S Grewal, et al.
Genetic Testing
|
March 31, 2007
Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systems
Karina Meden Sørensen, Cathrine Jespersgaard, Jens Vuust, et al.
Cardiovascular Research
|
February 5, 2003
Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations
Ole Havndrup, Henning Bundgaard, Paal Skytt Andersen, et al.
Gynecologic Oncology
|
September 27, 2005
P53 mutations in tissue from Danish ovarian cancer patients: from the Danish "MALOVA" ovarian cancer study
Estrid V S Høgdall, Susanne K Kjaer, Jan Blaakaer, et al.
European Journal of Human Genetics : EJHG
|
October 16, 2004
One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region
Lotte Hougs, Ole Havndrup, Henning Bundgaard, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Current Protocols in Human Genetics
|
April 23, 2008
Single-strand conformation polymorphism analysis using capillary electrophoresis
Lars Allan Larsen, Michael Christiansen, Jens Vuust, et al.
Aesthetic Plastic Surgery
|
March 11, 2005
Adverse reactions to injectable soft tissue permanent fillers
Lise Christensen, Vibeke Breiting, Martin Janssen, et al.
Human Mutation
|
April 4, 2003
Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening
Paal Skytt Andersen, Cathrine Jespersgaard, Jens Vuust, et al.
Human Mutation
|
January 29, 2003
High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method
Paal Skytt Andersen, Cathrine Jespersgaard, Jens Vuust, et al.
Ugeskrift for Laeger
|
October 31, 2006
[Screening for fragile X syndrome. International experiences]
Jens Vuust, Lars Allan Larsen, Karen Grønskov, et al.
FEMS Microbiology Letters
|
September 29, 2004
Identification and molecular characterization of the gene encoding coli surface antigen 20 of enterotoxigenic Escherichia coli
Håvard Valvatne, Hans Steinsland, Harleen M S Grewal, et al.
Genetic Testing
|
March 31, 2007
Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systems
Karina Meden Sørensen, Cathrine Jespersgaard, Jens Vuust, et al.
Cardiovascular Research
|
February 5, 2003
Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations
Ole Havndrup, Henning Bundgaard, Paal Skytt Andersen, et al.
Gynecologic Oncology
|
September 27, 2005
P53 mutations in tissue from Danish ovarian cancer patients: from the Danish "MALOVA" ovarian cancer study
Estrid V S Høgdall, Susanne K Kjaer, Jan Blaakaer, et al.
European Journal of Human Genetics : EJHG
|
October 16, 2004
One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region
Lotte Hougs, Ole Havndrup, Henning Bundgaard, et al.
Page
of 2